首页> 外文期刊>Bulletin of the Korean Chemical Society >Synthesis of Methyl(E)-2-Cyanomethylcinnamates Derived from Baylis-Hillman Acetates and Conversion into Several 4-Hydroxy-2-naphthoie Acids and Benzylidenesuccinimides
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Synthesis of Methyl(E)-2-Cyanomethylcinnamates Derived from Baylis-Hillman Acetates and Conversion into Several 4-Hydroxy-2-naphthoie Acids and Benzylidenesuccinimides

机译:衍生自Baylis-Hillman乙酸酯的(E)-2-氰基甲基肉桂酸甲酯的合成,并转化为几种4-羟基-2-萘甲酸和苯并亚苄基琥珀酰亚胺

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摘要

The Baylis-Hillman(BH)reaction has been developed enormously over the past few years due to its wide applicability towards formation of multifunctional derivatives,heterocycles3 and natural products.Aliphatic nitriles are potentially useful building block in organic synthesis due to the electron-withdrawing nature associated with the cyano group and the conversion of the cyano group into other functionalities.Much attention has recently been focussed on the S_N2' nucleophilic substitution of the Baylis-Hillman acetates.Among them only limited approaches to the cyanation of BH adducts are known in the literature.
机译:由于其在形成多功能衍生物,杂环化合物3和天然产物方面的广泛适用性,在过去的几年中,Baylis-Hillman(BH)反应得到了巨大的发展。由于吸电子的性质,脂族腈可能是有机合成中有用的结构单元。与氰基基团和氰基基团向其他官能团的转化有关。最近,人们集中注意力于Baylis-Hillman乙酸酯的S_N2'亲核取代。在这些方法中,仅已知有限的BH加合物氰化的方法。文学。

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